Public Display Solicitation
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Q24001462 Rapid HIV Antigen/Antibody Test Kits and Controls
- Solicitation Number
- Q24001462version: 01
- Status
- Cancelled
- Canceled Reason
- Quotes did not meet specifications or prices exceeded available funds.
- Department
- Health
- Division
- Communicable Disease and Public Health Nursing Division
- Canceled Date
- 02/23/2024 11:14 AM
- Islands (where the work/delivery is to be performed)
- Oahu
- Category
- Goods
- Release Date
- 01/30/2024
- Amendment Date
- 02/13/2024
- Amendment Reason
- Extended due date
- Offer Due Date & Time
- 02/20/2024 02:00 PM
- Description
- The Department of Health’s Harm Reduction Services Branch (HRSB) uses CDC awarded funding to purchase and distribute HIV testing kits and testing controls for rapid diagnosis and treatment of HIV and prevention of future infection. These kits are used for individuals at the highest risk of being infected with HIV.
HRSB orders, receives, and stores these kits on Oahu, and distributes them to community partners statewide for testing of individuals are high risk of HIV infection. This solicitation is for HIV test kits that meet the following specifications:
- The test kit must be a rapid, fourth generation point of care test.
- The test kit must detect both HIV-1/2 antibodies and HIV-1 p24 antigen.
- The test kit must be waived of Clinical Laboratory Improvement Amendments of 1988 (CLIA) requirements, and be approved by the US Food and Drug Administration (FDA) for use with fingerstick whole blood specimens.
- The test kit must yield results in 20 minutes or less.
- The test kit must be spill resistant if tipped over.
- The test kit shelf life must be at least 12 months.
- The rapid HIV antigen/antibody (Ag/Ab) controls must be compatible with the rapid HIV test kit to ensure its proper performance. - Contact Person
- Galvez, Danilyn
- danilyn.galvez@doh.hawaii.gov
- Phone
- 808-733-4387
- General Comments
- -Vendor must be registered and compliant in Hawaii Compliance Express (HCE)
- Procurement Officer
- Phillip Nguyen
- Attachments
- 103D-1 General Conditions.pdf
Direct all questions regarding this Solicitation, and any questions or Issues relating to the accessibility of this Solicitation (Including the appendices and exhibits to this Document, and any other document related to this Solicitation), to: Galvez, Danilyn.
Q24001462 Rapid HIV Antigen/Antibody Test Kits and Controls
#
Title
Quantity
Unit of Measure
Commodity Code
Commodity Code | Description |
---|---|
325413 | HIV test kits manufacturing |
- Quantity
- 3000
- Unit of Measure
- EACH
- Title
- 4th generation rapid antibody/antigen HIV tests
- Description
- - The test must be a rapid, fourth generation point of care test.
- The test must detect both HIV-1/2 antibodies and HIV-1 p24 antigen.
- The test must be waived of Clinical Laboratory Improvement Amendments of 1988 (CLIA) requirements, and be approved by the US Food and Drug Administration (FDA) for use with fingerstick whole blood specimens.
- The test must yield results in 20 minutes or less.
- The test must be spill resistant if tipped over.
- The test shelf life must be at least 12 months.
Commodity Code | Description |
---|---|
325413 | HIV test kits manufacturing |
- Quantity
- 10
- Unit of Measure
- EACH
- Title
- 4th generation rapid antibody/antigen HIV test controls
- Description
- -The rapid HIV antigen/antibody (Ag/Ab) controls must be compatible with the rapid HIV test kit to ensure quality assurance.
Direct all questions regarding this Solicitation, and any questions or Issues relating to the accessibility of this Solicitation (Including the appendices and exhibits to this Document, and any other document related to this Solicitation), to: Galvez, Danilyn.